SOPs

Procedure for handling of cultures & contaminated material

 STANDARD OPERATING PROCEDURE

Title :Procedure for handling of cultures & contaminated material

Department:Quality Control-Microbiology
  • OBJECTIVE
  • To lay down a procedure for handling of cultures & contaminated material.
  • SCOPE
  • This SOP is applicable for handling of cultures & contaminated material in microbiology laboratory .
  • RESPONSIBILITY
  • Officer / Executive- QC M – responsible for Implementation of SOP.
  • ACCOUNTABILITY
  • Manager – Quality Control
  • PROCEDURE
  • Used 2.5% Savlon /filtered 70% Isopropyl alcohol Solution to disinfect the spillage.
  • Wear hand gloves and spray /pour the disinfectant solution on the spilled medium/spilled culture.
  • If glassware is broken, pick up the broken glass pieces. Soak the broken glass pieces to the container meant for collection of broken glassware.
  • Swab the area of spillage to remove the media traces of medium/ microbial culture using a sterile non shedding duster soaked in disinfectant solution.
  • Wipe clean the area of spillage with a sterile non shedding duster soaked in disinfectant solution.
  • In case of aerosol has been created during spillage, fumigate the area on same time.
  •  In case of spillage of medium/ culture on LAF bench, clean the spillage with sterile non-shedding duster soaked in disinfectant solution. Switch on the UV light for one hour before start any activity in LAF unit.

 

  •         ABBREVIATION

SOP      –  Standard operating procedure

LAF      –  Laminar Air Flow

UV        – Ultra Violet

 

  • FORMAT-    Nil.

 

  • DISTRIBUTION LIST
Sr. No.Copy No.Department
Quality Assurance
Quality Control-Microbiology
VP – Plant & Operations

 

ABHA

Abha is the Author  of pharmaceutical guidance, she is a pharmaceutical professional having more than 22 years of rich experience in pharmaceutical field. During her career, she works in the quality assurance department with multinational companies i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd. During his experience, she faces many regulatorily audits i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda, Kenya, Tanzania, Zimbabwe. She is currently leading a regulatory pharmaceutical company as a Head Quality. You can join him by Email, Facebook, Google+, Twitter, and YouTube